Correction: Satam et al. Next-Generation Sequencing Technology: Current Trends and Advancements. Biology 2023, 12, 997

We are very thankful to the commentator for pointing out the issues in the review article by Satam et al [...].

We are very thankful to the commentator for pointing out the issues in the review article by Satam et al. [1].As noted by the commentator, there were a few discrepancies related to the information about the PacBio system in the review article by Satam et al., as discussed below.
The commentator highlighted the point in the original article regarding the higher error rate of long-read sequencing compared to short-read sequencing.We presented this as a general statement for long-read sequencing technologies, without specifically mentioning PacBio.We acknowledge the updated information and the references cited by the commentator.After considering the references cited by the commentator and the study from the Association of Biomolecular Resource Facilities (ABRF), we agree with the updated information provided by the commentator that PacBio CCS has the lowest error rate among all sequencing technologies.
The commentator identified an error in Figure 2 and Table 1 of the original article.We appreciate the raised comment and acknowledge that it was an unintentional typographical mistake.In the subsequent paragraph of the original article, where we compare short-read and long-read sequencing, we used the term 'PCR-Free'.We apologize for the typographical error in Figure 2 of the article, which has now been rectified (see the corrected figure below).Furthermore, we have also corrected this information in      The error rate can spike up to 15%, especially with low-complexity sequences.Compared to short-read sequencers, it has a lower read accuracy.
[ 5,19,30] The commentator drew attention to the issue regarding the read length of PacBio as stated in the original article.We originally mentioned a read length of 10-16 kb.We acknowledge that the reference we cited was old, and the references cited by the commentator for this are the most recent and updated, suggesting a read length of 15-25 kb.Therefore, we revised our statement accordingly that the average read length of the PacBio system is 10-25 kb (See corrected Table 1

above).
The commentator highlighted statements related to PacBio SMRT sequencing, including 'in wells where high processive DNA is prebound', 'fluorescently labeled nucleotides which upon incorporation emit a fluorescent signal', and 'the molecule quickly diffuses' (Table 1).We acknowledge that these statements were not correctly phrased.The information was sourced from a review article by Mantere et al. which describes these details using similar terms, such as 'pre-bound polymerase' and 'incorporation of the labeled bases,' in the technical summary of SMRT in their review article.In light of the raised comments and for better clarity for readers, we have revised these statements (See Table 1) In the context of the comment on the low throughput of the PacBio SMRT system, we accept that appropriate references were not quoted; we apologize for that.In light of the comment and the reference cited by the commentator, we revise our statement that the PacBio Pac Bio SMRT system has a high throughput.
The commentator has pointed out that our statement regarding PacBio SMRT sequencing having 'low flow cell success' (Table 1 of the original article) is inaccurate.He clarifies that PacBio SMRT sequencing does not utilize flow cells, and there is no flow of any reagents during the sequencing reaction.We apologize if this information was not accurately presented in the original article's table, and we want to clarify that we did not intend to damage PacBio's reputation.After carefully evaluating comments and cited references, we have revised these statements in the table (see above Table 1).
The commentator highlighted the statements on PacBio Onso short-read sequencing.We initially mentioned, "The minimum data are 80 GB with 200 cycles, which necessitates a higher sample requirement (Table 1).After careful examination of the facts and comments, we agree that neither the minimum amount of data nor the number of cycles dictate sample input requirements, as SBB chemistry can utilize PCR amplification just like other shortread technologies.The authors accept the comment made on the relation between the sample input requirement and data output.We agree with the fact that Onso systems work with as low as 10 ng input.

Figure 2 .
Figure 2. Overview of various NGS technologies with different platforms and principles.

Figure 2 .
Figure 2. Overview of various NGS technologies with different platforms and principles.

Table 1 .
Different generations of NGS platforms.